Seroatlas · Human Serome Atlas

CXCL13

C-X-C motif chemokine 13

Also known as: ANGIE, ANGIE2, BCA-1, BLC, BLR1L, CXL13_HUMAN, SCYB13

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
O43927
Gene
CXCL13
Ensembl
ENSG00000156234
Chromosome
4
Canonical length
109 aa
Protein class
Cancer-related genes, Predicted secreted proteins
Secretome location
Secreted to blood

OverviewNCBI Gene

B lymphocyte chemoattractant, independently cloned and named Angie, is an antimicrobial peptide and CXC chemokine strongly expressed in the follicles of the spleen, lymph nodes, and Peyer's patches. It preferentially promotes the migration of B lymphocytes (compared to T cells and macrophages), apparently by stimulating calcium influx into, and chemotaxis of, cells expressing Burkitt's lymphoma receptor 1 (BLR-1). It may therefore function in the homing of B lymphocytes to follicles. [provided by RefSeq, Oct 2014]

Canonical amino-acid sequenceUniProt

109 residues, UniProt reviewed canonical sequence.

>O43927|CXCL13
     1  MKFISTSLLL MLLVSSLSPV QGVLEVYYTS LRCRCVQESS VFIPRRFIDR IQILPRGNGC
    61  PRKEIIVWKK NKSIVCVDPQ AEWIQRMMEV LRKRSSSTLP VPVFKRKIP

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CXCL13 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.47
Highest tissue expression
506 nTPM

Expression across tissuesHPA

Tissue

  • lymph node: 506 nTPM
  • tonsil: 428 nTPM
  • spleen: 298 nTPM
  • appendix: 124 nTPM
  • stomach: 34 nTPM
  • urinary bladder: 30 nTPM

Single-cell type

  • breast hormone-responsive cells: 509 nCPM
  • decidual stromal cells: 212 nCPM
  • endometrial stromal cells: 76 nCPM
  • t-cells: 25 nCPM
  • hepatocytes: 25 nCPM
  • platelets: 17 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • medulla oblongata: 2.2 nTPM
  • basal ganglia: 0.7 nTPM
  • cerebellum: 0.7 nTPM
  • spinal cord: 0.7 nTPM
  • cerebral cortex: 0.4 nTPM
  • white matter: 0.2 nTPM

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
0.52
gnomAD pLI
0.83
gnomAD missense Z
0.58
DepMap mean gene effect
0.11
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CXCL13 as an antibody target. Whether an autoantibody or antibody against CXCL13 could matter depends on whether native CXCL13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CXCL13 is annotated as secreted, so native CXCL13 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label CXCL13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CXCL13. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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